Items where Author is "Alipour, P."

Article

(2022) Next-generation sequencing reveals a novel pathogenic variant in the ATM gene. Int J Neurosci. pp. 558-562. ISSN 0020-7454

(2021) Next-generation sequencing reveals a novel pathogenic variant in the ATM gene. Int J Neurosci. pp. 1-5. ISSN 0020-7454

(2019) A pathogenic variant in SLC26A4 is associated with Pendred syndrome in a consanguineous Iranian family. Int J Audiol. pp. 1-7. ISSN 1708-8186 (Electronic) 1499-2027 (Linking)

(2017) A novel pathogenic variant in an Iranian Ataxia telangiectasia family revealed by next-generation sequencing followed by in silico analysis. Journal of the Neurological Sciences. pp. 212-216. ISSN 0022-510X

(2016) Genetic linkage analysis of DFNB40 and DFNB48 loci in families with autosomal recessive non-syndromic hearing loss (ARNSHL) from western provinces of Iran. Journal of Isfahan Medical School. ISSN 10277595 (ISSN)

(2015) Genetic linkage analysis of the DFNB63 locus in families with autosomal recessive nonsyndromic hearing loss from Hamadan and Kohgiluyeh and Boyer-Ahmad Provinces, Iran. Journal of Isfahan Medical School. pp. 1308-1317. ISSN 10277595 (ISSN)